CLRES 2050 Live aims to enhance student's ability to think about the ethical dimensions of research, especially research involving human subjects, and to participate thoughtfully and knowledgeably in the ethical design and review of research protocols. By the end of the course, students should be able to: (1) Describe the historical context for today's heightened scrutiny of clinical research, (2) Identify and explain the basic concepts, values, and potential ethical conflicts associated with the conduct of human subjects research, (3) Define the elements of scientific misconduct, (4) Demonstrate a commitment to integrity in the conduct of scientific research, (5) Demonstrate a commitment to advocate for the rights and welfare of human research subjects, (6) Analyze a research protocol from the ethical point of view according to criteria developed by federal regulatory agencies and local Institutional Review Boards, (7) Explain a scientific research protocol in language that promotes laypeople's understanding sufficient to provide meaningful informed consent and (8) Demonstrate communication skills adequate to obtain a potential research subject's meaningful informed consent.
Breadcrumb
- Academics
- Pharmaceutical Science Graduate Programs
- PhD in Pharmaceutical Sciences
- Clinical Pharmaceutical Scientist Program
- Curriculum
- Ethics and Regulation of Clinical Research (CLRES 2050)